MedPath

Treatment of Insomnia in Primary Care Study

Not Applicable
Recruiting
Conditions
Insomnia Chronic
Interventions
Behavioral: Treatment as usual
Behavioral: Sleep School
Registration Number
NCT06149273
Lead Sponsor
University of Turku
Brief Summary

The goal of this clinical trial is to learn about insomnia treatment among primary care patients with chronic insomnia.

The main question it aims to answer is:

• Does Sleep School (a therapy for insomnia) work well to decrease harm of insomnia? Participants will attend a group therapy intervention once a week for six weeks.

Researchers will compare Sleep School to treatment as usual (short counselling by an educated nurse) to see if the Sleep School works better than treatment as usual in decreasing the harm of insomnia.

Detailed Description

Not available

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
250
Inclusion Criteria
  • Insomnia severity index (ISI) score at least 8
  • insomnia symptoms present at least for 3 months
Exclusion Criteria
  • diagnosed dementia based on medical records
  • acute suicidality
  • acute psychotic symptoms

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Treatment as usualTreatment as usualParticipants receive short counselling about insomnia at the enrollment visit.
Sleep SchoolSleep SchoolParticipants attend the Sleep School once a week for six weeks.
Primary Outcome Measures
NameTimeMethod
Mean Change from Baseline in Insomnia Severity Index (ISI) score at 8 weeksBaseline and Week 8

The ISI is a validated self-report tool for assessing the severity, and impact of current insomnia symptoms. It consists of 7 Likert-scale questions with a total score ranging from 0 to 28 (with higher scores indicating more severe insomnia). Change = Week 8 score - Baseline score.

Secondary Outcome Measures
NameTimeMethod
Mean change from Baseline in Patient Health Questionnaire 9 (PHQ-9) at 8 weeksBaseline and Week 8

PHQ-9 is a validated self-administered instrument assessing each of the 9 Diagnostic and Statistical Manual of Mental Disorders (DSM)-IV criteria for depression as 0 (not at all) to 3 (nearly every day), and the severity of depression. Possible scores range from 0 to 27. Change = Week 8 score - Baseline score.

Mean change from Baseline in EUROHIS Quality of Life 8-item Index at 8 weeksBaseline and Week 8

EUROHIS Quality of Life 8-item Index is a validated instrument for the assessment of general quality of life. There are altogether eight questions about the general, physical, psychological, social, and environmental aspects of quality of life. Every question is scored from 1 (very poor) to 5 (very good). All scores can be added together and divided by 8 (the sum of the questions) to obtain the EUROHIS-QOL mean score. Change = Week 8 score - Baseline score.

Mean change from Baseline in Work Ability Score (WAS) at 8 weeksBaseline and Week 8

The WAS is the first item of the Work Ability Index (WAI), a validated instrument for the assessment of work ability. WAS is a single question "What is your current work ability compared to your lifetime best?" It has a 0-10 response scale, where 0 stands for "completely unable to work" and 10 stands for "work ability at its best." The WAS has been shown to have a strong association with the WAI and is reliable in evaluating work ability. Change = Week 8 score - Baseline score.

Trial Locations

Locations (1)

University of Turku

🇫🇮

Turku, Finland

© Copyright 2025. All Rights Reserved by MedPath